Wikipedia

C20orf27

UPF0687 protein C20orf27 is a protein that in humans is encoded by the C20orf27 gene.[5][6] It is expressed in the majority of the human tissues. One study on this protein revealed its role in regulating cell cycle, apoptosis, and tumorigenesis via promoting the activation of NFĸB pathway.[7]

C20orf27
Identifiers
AliasesC20orf27, chromosome 20 open reading frame 27
External IDsMGI: 1914576; HomoloGene: 41660; GeneCards: C20orf27; OMA:C20orf27 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

54976

67326

Ensembl

ENSG00000101220

ENSMUSG00000027327

UniProt

Q9GZN8

Q9D1K7

RefSeq (mRNA)

NM_001039140
NM_001258429
NM_001258430
NM_017874

NM_026091
NM_001311138
NM_001361375

RefSeq (protein)

NP_001034229
NP_001245358
NP_001245359

NP_001298067
NP_080367
NP_001348304

Location (UCSC)Chr 20: 3.75 – 3.77 MbChr 2: 130.99 – 131 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Gene

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The UPF0687 Protein C20orf27 has four other aliases, Chromosome 20 Open Reading Frame 27,[8] Hypothetical Protein LOC54976,[9] C20orf27, and FLJ20550. It is located on the minus strand at 20p13.[8] It consists of 7 exons and 12 introns. This most updated annotation shows that gene C20orf27 starts at 3,753,499 bp to 3,768,388 bp on Chromosome 20.

Transcription

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Known isoforms

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The C20orf27 gene has 5 transcript isoforms, C20orf27 transcript variant 1, C20orf27 transcript variant 2, C20orf27 transcript variant 3, and C20orf27 transcript variant 4.[8]

Transcript variant 1 encodes for the longest protein isoform, with a size of 1327 bases and 6 exons.[10]

Transcript variant 2 maintains the reading frames and 6 exons compared to transcript variant 1, but it has an alternative spliced site in the coding region.[8] It has a size of 1252 bases.[11]

Transcription variant 3 has a size of 1706 bases and 6 exons.[12] This variant has an alternative spliced site in the coding region and differs in the 5’ UTR, but it still maintains the reading frame seen in transcript variant 1.[8] Despite their differences in size, variant 2 and variant 3 encodes the same protein isoform and this second protein isoform is shorted than the protein isoform encoded by transcript variant 1.

Transcript variant 4 has a size of 1457 bases with 6 exons.[13] Compared to variant 1, it uses an alternative 5’-most exon and an alternative splice site.[8] Because of the presence of an upstream ORF that is predicted to interfere with translation of this variant, the transcription variant 4 does not encode any protein.

The information on transcript variant X1 comes from GRCh38.p13 Primary Assembly.[14] This variant has a size of 1195 bases, and the number of exons in this variant remains unknown.

Proteins

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Physical features

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Conceptional translation of C20orf27. Labeled are start and stop codons, exon spliced regions, polyadrenylation signals, and ribosome binding site. Bold are conserved amino acids.

The human gene C20orf27 has three known isoforms.[8]

Isoform 1 has 199 amino acid residues and a domain named DUF4517. Isoform 2 has 174 amino acid residues, and isoform X1 has 154 amino acid residues. All three isoforms contain the same domain DUF4517. The function of domain DUF4517 requires future research.

The predicted isoelectric point of unmodified protein C20orf27 is 6.89.[15]

The percentage of each amino acid residue is about its average percentage among human proteins.[16] Overall, the positively charged amino acid residues in human protein C20orf27 outnumbers the negatively charged amino acid residues. Protein C20orf27 has no high scoring hydrophobic regions, no highly charged regions, and no transmembrane regions.

SPAS predicts two repetitive structures. The first repetitive structure is amino acid alphabet structures with a core block length of 4. The total number of this structure in human protein C20orf27 is 15. The second repetitive structure is an 11-letter reduced alphabet structure with a core block length of 8. This charged alphabet structure predicts to appear 8 times in human protein C20orf27. There are no predicted clusters of amino acid multiples.

Post-translation modifications

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The predicted molecular weight of C20orf27 is 21.6 kDa.[16] A Western Blot binding pattern on protein C20orf27 with its polyclonal antibody reveals that the experimental molecular weight of protein C20orf27 is about 22 kDa.[17] This suggests that there are relatively few post-translation modifications on protein C20orf27.

There is no predicted signal peptide or cleavage site.

 
Predicted phosphorylation sites in protein C20orf27 by NetPhos 3.1

There are many predicted phosphorylation sites along the sequence of protein C20orf27, including four sites for protein kinase A (PKA), two sites for protein kinase C (PKC), three sites for casein kinase 2 (CKII), one site for ribosomal S6 kinase (RSK), one site for cGMP-dependent protein kinase or Protein Kinase G (PKG), and one site for ataxia-telangiectasia mutated (ATM) serine/threonine protein kinase.[18]

Protein C20orf27 is predicted to have other post-translation modification sites including five palmitoylation sites,[19] one c-mannosylation site,[20] and two sumoylation sites.[21]

Structure

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Three stretches of beta sheet from amino acid 62 to 67, 76 to 87, and 92 to 100 are predicted with the highest confidence using CFSSP[22] and Phyre2.[23] A model predicted by I-TASSER[24] shows that the tertiary structure of human protein C20orf27 is a combination of many beta sheets. This confirms the predictions made by CFSSP and Phyre2.

Subcellular Localization

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This protein is expected to be found in cytosol and nucleus, but not in nuclei.[25] Additional computational analysis predicts that this protein is most likely to be in cytosol.[26]

Expression

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Protein C20orf27 is expressed ubiquitously throughout different human tissues. Microarray-assessed tissue expression pattern suggests caudate nucleus has the highest expression of protein C20orf27.[27]

Other than caudate nucleus, protein C20orf27 expression measure ranks at the top 25% among 100 proteins in pons, fetal brain, BM- CD105+ endothelial, BM- CD34+, bone marrow, adipocyte, uterus corpus, 721 BLymphoblast, PB- CD56+NK cells, BM- CD33+ myeloid, colorectal adenocarcinoma, leukemia chronic Myelogenous K-562, leukemia lymphoblastic (MOLT-4), and leukemia promyelocytic-HL-60.

In situ hybridization data has shown that the expression of C20orf27 in airway epithelial cells (AECs) can be correlated to chronic lung diseases.[28] After AECs are treated with IL-13, which is a cytokine expressed by CD4 T helper cells, AECs begin to secrete excess mucous, and excess mucous secretion in the airway is a mark of chronic lung diseases.

Regulation of expression

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Gene level expression

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C20orf27 Promoter Diagram

There are three promoter regions in gene C20orf27.

Five transcription factors that bind to the promoter region of gene C20orf27[29] have been discovered, including MITF, JUN, ZNF282, FOXA1, and TCF7L2.

Using genomatix, more transcription factor binding sites are predicted.[30] Transcription binding matrix, like EGR/nerve growth factor induced protein C & related factors, GC-Box factors SP1/GC, Krueppel like transcription factors, Myc associated zinc fingers, vertebrate homologues of enhancer of split complex, E-box binding factors, E2F-myc activator/cell cycle regulator, and BED subclass of zinc-finger proteins, are predicted to give the highest matrix similarity.

Transcript level regulation

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The 3' end of C20orf27 mRNA including all the predicted microRNA binding sites, predicted mRNA binding protein binding sites, and the sequence of three predicted stem loops.

Predicted miRNA binding sites in 3' end of C20orf27 mRNA which sequences are also conserved evolutionarily are hsa-miR-7856-5p, hsa-miR-671-5p, hsa-miR-4768, hsa-miR-6791-3p, hsa-miR-6829-3p, hsa-miR-548d-3p, hsa-miR-548-3p, hsa-miR-548z, and hsa-miR-548h-3p.[31]

 
Predicted C20orf27 mRNA secondary structure

The formation of three stem loops is conserved in different predicted models.[32] The three stem loops start from the 5' end of C20orf27 mRNA base 1 to base 27, base 56 to base 74, and base 116 to base 130.

The mRNA of C20orf27 has about 23 predicted mRNA binding protein binding sites which sequences are also conserved in evolution.[33] The names of these mRNA binding proteins are BRUNOL5, BRUNOL6, PCBP2, TARDBP, MBNL1, CUG-BP, PCBP3, PTBP1, RBM5, SRSF1, HNRNPH2, FMR1, HNRNPF, LIN28A, CPEB4, HNRNPC, HNRNPCL1, HNRNPM, HuR, RALY, PABPC1, PABPC4, SART3, and SRSF10.

Function and clinical significance

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Interacting proteins

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Interactors of protein C20orf27 found in Y2H screen are replicase polyprotein 1ab from coronavirus,[34] RAIYL,[35] PHKB,[35] FERMT2[36] from human. The function of replicase polyprotein 1ab is transcribing and replicating viral RNAs, and it contains the proteinases responsible for the cleavages of the polyprotein.[37] The function of RAIYL,[35] PHKB,[35] and FERMT2[36] remain unknown.

Other interactors that discovered by pull-down assays include PPP1CA,[38] PPP1CC,[38] PPP1CB,[39] PPP1R7,[39] PSME3,[40] RBFOX2,[40] and DMWD.[40] Interactors PPP1CA, PPP1CB, PPP1CC, and PPP1R7 have similar functions. They involve in the regulation of a variety of cellular processes, such as cell division, glycogen metabolism, muscle contractility, protein synthesis, and HIV-1 viral transcription.[41][42][43][44] PSME3 facilitates the MDM2-p53/TP53 interaction which promotes ubiquitination- and MDM2-dependent proteasomal degradation of p53/TP53, limiting its accumulation and resulting in inhibited apoptosis after DNA damage, and might play a role in cell cycle regulation.[45][46][47][48][49][50][51] RBFOX2 regulates alternative splicing events by binding to 5'-UGCAUGU-3' elements.[52] The function of DMWD is unknown.

The above evidence suggests protein C20orf27 plays a role in cell cycle regulation, cell proliferation and differentiation, and cell survival.

Clinical significance

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Human protein C20orf27 and its variants have not been discovered to be associated with any diseases or disorders.

Homology and evolution history

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Paralogs

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There are no known paralogs.[8]

Orthologs

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There are about 281+ known orthologs for this gene, ranging from primates to invertebrates.[8]

 
Graph showing gene C20orf27 rate of divergence compared to cytochrome c and fibrinogen alpha.

The closest related orthologs are selected from primates and mammals, and the sequence similarity ranks from 75% to 100%. The moderately related orthologs are selected from fishes and birds, and the sequence similarity ranks from 55% to 75%. The most distantly related orthologs are selected from invertebrates and trichoplax, and the sequence similarity ranks from 40% to 55%. The conserved amino acids are bold in the conceptional translation diagram.

Gene name Genus and Species taxonomic group Common Names Accession Num. Protein Length Seq Identity Seq Similarity MYA
C20orf27 Homo sapiens Primates Human NP_001034229.1 199 aa 100% 100% 0
C20orf27 Macaca mulatta Primates Old World Monkey AFE71948.1 197 aa 98.50% 99% 29.44
C20orf27 Mus musculus Rodentia House mouse NP_001298067.1 177 aa 79.40% 82.90% 90
C20orf27 Rhinolophus ferrumequinum Chiroptera Greater horseshoe bat XP_032951391.1 174 aa 82.40% 85.40% 96
C20orf27 Condylura cristata Eulipotyphla Star-nosed mole XP_012583921.1 184 aa 76.60% 79.90% 96
C20orf27 Dromaius novaehollandiae Casuariiformes Emu XP_025975497.1 174 aa 65.30% 72.90% 312
C20orf27 Gopherus evgoodei Testudines Gopher Tortoises XP_030419106.1 176 aa 61.80% 73.90% 312
C20orf27 Strigops habroptila Psittaciformes Kakapo XP_030348224.1 174 aa 59.30% 70.40% 312
C20orf27 Thamnophis elegans Scaled reptiles Western terrestrial garter snake XP_032094251.1 174 aa 56.80% 68.30% 312
C20orf27 Taeniopygia guttata Passeriformes Zebra finch NP_001232719.1 176 aa 56.70% 67.50% 312
C20orf27 Xenopus tropicalis Frogs Western clawed frog NP_001007504.1 174 aa 59.30% 72.40% 351.8
C20orf27 Scophthalmus maximus Pleuronectiformes Turbot AWP06390.1 179 aa 29.70% 43.20% 435
C20orf27 Callorhinchus milii Chimaera Australian ghostshark XP_007906148.1 179 aa 54.00% 63.90% 473
C20orf27 Petromyzon marinus Petromyzontiformes Sea lamprey XP_032806447.1 173 aa 47.60% 55.80% 615
C20orf27 Anneissia japonica Comatulida comasterids XP_033124803.1 184 aa 26.60% 46.30% 684
C20orf27 Ixodes scapularis Ixodida Deer tick XP_002403181.1 165 aa 28.80% 44.20% 797
C20orf27 Limulus polyphemus Xiphosura Atlantic horseshoe crab XP_022257482.1 173 aa 28.80% 44.50% 797
C20orf27 Crassostrea gigas Ostreida Pacific oyster XP_011438297.1 162 aa 24.90% 44.00% 797
C20orf27 Drosophila subobscura Fly Fruit Fly XP_034657203.1 179 aa 24.70% 37.70% 797
C20orf27 Nematostella vectensis Sea anemone Starlet sea anemone XP_001627979.1 169 aa 30.30% 43.30% 824
C20orf27 Trichoplax Trichoplax Trichoplax RDD38604.1 166 aa 22.3% 40.0% 1017

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000101220 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000027327 – Ensembl, May 2017
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  26. ^ PSORT: a portal to protein subcellular localization resources. Retrieved on 2020-8-02.
  27. ^ NCBI (National Center for Biotechnology Information) GEO Profile entry on C20orf27 gene https://www.ncbi.nlm.nih.gov/geo/tools/profileGraph.cgi?ID=GDS596:50314_i_at. Retrieved on 2020-8-01.
  28. ^ NCBI (National Center for Biotechnology Information) GEO Profile entry on C20orf27 gene. Retrieved on 2020-8-01.
  29. ^ SPP (The Signaling Pathway Project) transcription factors report on C20orf27 gene. Retrieved on 2020-8-01.
  30. ^ "Genomatix - NGS Data Analysis & Personalized Medicine". www.genomatix.de. Archived from the original on 2001-02-24. Retrieved 2020-08-02.
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  47. ^ Li J, Gao X, Joss L, Rechsteiner M (June 2000). "The proteasome activator 11 S REG or PA28: chimeras implicate carboxyl-terminal sequences in oligomerization and proteasome binding but not in the activation of specific proteasome catalytic subunits". Journal of Molecular Biology. 299 (3): 641–54. doi:10.1006/jmbi.2000.3800. PMID 10835274.
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Further reading

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  • Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, et al. (October 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.
  • Gevaert K, Goethals M, Martens L, Van Damme J, Staes A, Thomas GR, Vandekerckhove J (May 2003). "Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides". Nature Biotechnology. 21 (5): 566–9. doi:10.1038/nbt810. PMID 12665801. S2CID 23783563.
  • Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (October 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
  • Maruyama K, Sugano S (January 1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
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